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For: Nehra N, Tittal RK, Ghule VD. 1,2,3-Triazoles of 8-Hydroxyquinoline and HBT: Synthesis and Studies (DNA Binding, Antimicrobial, Molecular Docking, ADME, and DFT). ACS Omega 2021;6:27089-100. [PMID: 34693129 DOI: 10.1021/acsomega.1c03668] [Cited by in Crossref: 9] [Cited by in F6Publishing: 11] [Article Influence: 4.5] [Reference Citation Analysis]
Number Citing Articles
1 Kaushik R, Nehra N, Novakova V, Zimcik P. Near-Infrared Probes for Biothiols (Cysteine, Homocysteine, and Glutathione): A Comprehensive Review. ACS Omega 2023;8:98-126. [PMID: 36643462 DOI: 10.1021/acsomega.2c06218] [Reference Citation Analysis]
2 Kumar V, Lal K, Kumar A, Tittal RK, Singh MB, Singh P. Efficient synthesis, antimicrobial and molecular modelling studies of 3-sulfenylated oxindole linked 1,2,3-triazole hybrids. Res Chem Intermed 2022. [DOI: 10.1007/s11164-022-04933-0] [Reference Citation Analysis]
3 Mokariya JA, Rajani DP, Patel MP. 1,2,4‐Triazole and benzimidazole fused dihydropyrimidine derivatives: Design, green synthesis, antibacterial, antitubercular, and antimalarial activities. Archiv der Pharmazie 2022. [DOI: 10.1002/ardp.202200545] [Reference Citation Analysis]
4 Chalkha M, Nour H, Chebbac K, Nakkabi A, Bahsis L, Bakhouch M, Akhazzane M, Bourass M, Chtita S, Bin Jardan YA, Augustyniak M, Bourhia M, Aboul-Soud MAM, El Yazidi M. Synthesis, Characterization, DFT Mechanistic Study, Antimicrobial Activity, Molecular Modeling, and ADMET Properties of Novel Pyrazole-isoxazoline Hybrids. ACS Omega 2022;7:46731-44. [PMID: 36570248 DOI: 10.1021/acsomega.2c05788] [Reference Citation Analysis]
5 Haroun M. Review on the Developments of Benzothiazole-containing Antimicrobial Agents. Curr Top Med Chem 2022;22:2630-59. [PMID: 36503470 DOI: 10.2174/1568026623666221207161752] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
6 Deng C, Yan H, Wang J, Liu K, Liu B, Shi Y. 1,2,3-Triazole-containing hybrids with potential antibacterial activity against ESKAPE pathogens. European Journal of Medicinal Chemistry 2022;244:114888. [DOI: 10.1016/j.ejmech.2022.114888] [Reference Citation Analysis]
7 Yadav A, Kaushik CP. Synthesis and antibacterial evaluation of sulfonamide bridged disubstituted 1,2,3-triazoles. Synthetic Communications 2022. [DOI: 10.1080/00397911.2022.2141126] [Reference Citation Analysis]
8 Lengerli D, Ibis K, Nural Y, Banoglu E. The 1,2,3-triazole 'all-in-one' ring system in drug discovery: a good bioisostere, a good pharmacophore, a good linker, and a versatile synthetic tool. Expert Opin Drug Discov 2022;17:1209-36. [PMID: 36164263 DOI: 10.1080/17460441.2022.2129613] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
9 Malah TE, Hegab MI, Awad HM, Abdelrahman MT, Abdel-megeid FM, Shamroukh AH, Mageid REA, Nour HF. Benzothiazole-tethered 1,2,3-triazoles: Synthesis, antimicrobial, antioxidant, and molecular docking studies. Journal of Molecular Structure 2022;1266:133417. [DOI: 10.1016/j.molstruc.2022.133417] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
10 Amariucai-mantu D, Mangalagiu V, Bejan I, Aricu A, Mangalagiu II. Hybrid Azine Derivatives: A Useful Approach for Antimicrobial Therapy. Pharmaceutics 2022;14:2026. [DOI: 10.3390/pharmaceutics14102026] [Reference Citation Analysis]
11 El-dershaby NH, El-hawash SA, Kassab SE, Daabees HG, Abdel Moneim AE, El-miligy MMM. Rational Design and Synthesis of New Selective COX-2 Inhibitors with In Vivo PGE2-Lowering Activity by Tethering Benzenesulfonamide and 1,2,3-Triazole Pharmacophores to Some NSAIDs. Pharmaceuticals 2022;15:1165. [DOI: 10.3390/ph15101165] [Reference Citation Analysis]
12 Khan A, Naaz F, Basit R, Das D, Bisht P, Shaikh M, Lone BA, Pokharel YR, Ahmed QN, Parveen S, Ali I, Singh SK, Chashoo G, Shafi S. 1,2,3-Triazole Tethered Hybrid Capsaicinoids as Antiproliferative Agents Active against Lung Cancer Cells (A549). ACS Omega. [DOI: 10.1021/acsomega.2c03325] [Reference Citation Analysis]
13 Veeranna D, Ramdas L, Ravi G, Bujji S, Thumma V, Ramchander J. Synthesis of 1,2,3‐Triazole Tethered Indole Derivatives: Evaluation of Anticancer Activity and Molecular Docking Studies. ChemistrySelect 2022;7. [DOI: 10.1002/slct.202201758] [Reference Citation Analysis]
14 Rana M, Faizan MI, Dar SH, Ahmad T, Rahisuddin. Design and Synthesis of Carbothioamide/Carboxamide-Based Pyrazoline Analogs as Potential Anticancer Agents: Apoptosis, Molecular Docking, ADME Assay, and DNA Binding Studies. ACS Omega. [DOI: 10.1021/acsomega.2c02033] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
15 Miao Q, Xu Y, Miao T, Xu L. Theoretical insights and design of Ru(II)-based complexes with DNA-photocleavage properties. Journal of the Indian Chemical Society 2022;99:100320. [DOI: 10.1016/j.jics.2021.100320] [Reference Citation Analysis]
16 Reetu R, Garg A, Roy KK, Roy A, Gupta S, Malakar CC. In-silico studies for targeting PPARγ for the Type II Diabetes Mellitus. Materials Today: Proceedings 2022;57:44-48. [DOI: 10.1016/j.matpr.2022.01.299] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]